PH26142A - Use of benzimidazole derivatives as yield promoters - Google Patents

Use of benzimidazole derivatives as yield promoters Download PDF

Info

Publication number: PH26142A
Authority: PH; Philippines
Prior art keywords: stands; hydrogen; alkyl; formula; halogen
Prior art date: 1988-01-05

Application number

PH38006A

Other languages

English (en)

Inventor

Gerhard Bonse

Werner Hallenbach

Hans Lindel

Friedrich Berschauer

Original Assignee

Bayer Ag

Priority date (The priority date is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the date listed.)

1988-01-05

Filing date

1989-01-05

Publication date

1992-03-18

1989-01-05 Application filed by Bayer Ag filed Critical Bayer Ag

1992-03-18 Publication of PH26142A publication Critical patent/PH26142A/en

Links

125000003785 benzimidazolyl group Chemical class N1=C(NC2=C1C=CC=C2)* 0.000 title claims 5
229940058303 antinematodal benzimidazole derivative Drugs 0.000 title 1
150000001875 compounds Chemical class 0.000 claims description 93
229910052739 hydrogen Inorganic materials 0.000 claims description 50
239000001257 hydrogen Substances 0.000 claims description 50
238000000034 method Methods 0.000 claims description 47
125000000217 alkyl group Chemical group 0.000 claims description 43
229910052736 halogen Inorganic materials 0.000 claims description 30
150000002367 halogens Chemical class 0.000 claims description 30
150000002431 hydrogen Chemical class 0.000 claims description 30
UFHFLCQGNIYNRP-UHFFFAOYSA-N Hydrogen Chemical compound [H][H] UFHFLCQGNIYNRP-UHFFFAOYSA-N 0.000 claims description 20
241001465754 Metazoa Species 0.000 claims description 19
150000003839 salts Chemical class 0.000 claims description 15
125000002496 methyl group Chemical group [H]C([H])([H])* 0.000 claims description 10
125000001188 haloalkyl group Chemical group 0.000 claims description 9
230000001737 promoting effect Effects 0.000 claims description 9
125000003545 alkoxy group Chemical group 0.000 claims description 8
125000002887 hydroxy group Chemical group [H]O* 0.000 claims description 8
125000003118 aryl group Chemical group 0.000 claims description 5
125000001997 phenyl group Chemical group [H]C1=C([H])C([H])=C(*)C([H])=C1[H] 0.000 claims description 4
125000002947 alkylene group Chemical group 0.000 claims description 3
HZAXFHJVJLSVMW-UHFFFAOYSA-N 2-Aminoethan-1-ol Chemical compound NCCO HZAXFHJVJLSVMW-UHFFFAOYSA-N 0.000 claims description 2
229910052799 carbon Inorganic materials 0.000 claims description 2
125000000753 cycloalkyl group Chemical group 0.000 claims 2
239000011149 active material Substances 0.000 claims 1
125000002252 acyl group Chemical group 0.000 claims 1
125000004438 haloalkoxy group Chemical group 0.000 claims 1
125000001415 nervonoyl group Chemical group O=C([*])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])/C([H])=C([H])\C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])[H] 0.000 claims 1
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CCGKOQOJPYTBIH-UHFFFAOYSA-N ethenone Chemical compound C=C=O CCGKOQOJPYTBIH-UHFFFAOYSA-N 0.000 description 3
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TYQCGQRIZGCHNB-JLAZNSOCSA-N l-ascorbic acid Chemical compound OC[C@H](O)[C@H]1OC(O)=C(O)C1=O TYQCGQRIZGCHNB-JLAZNSOCSA-N 0.000 description 3
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229960001760 dimethyl sulfoxide Drugs 0.000 description 1
230000009977 dual effect Effects 0.000 description 1
230000000694 effects Effects 0.000 description 1
239000000839 emulsion Substances 0.000 description 1
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DECIPOUIJURFOJ-UHFFFAOYSA-N ethoxyquin Chemical compound N1C(C)(C)C=C(C)C2=CC(OCC)=CC=C21 DECIPOUIJURFOJ-UHFFFAOYSA-N 0.000 description 1
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150000002430 hydrocarbons Chemical class 0.000 description 1
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238000004519 manufacturing process Methods 0.000 description 1
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MMLNFWPLMKLQFK-UHFFFAOYSA-N methyl 4-(2-oxopropyl)benzoate Chemical compound COC(=O)C1=CC=C(CC(C)=O)C=C1 MMLNFWPLMKLQFK-UHFFFAOYSA-N 0.000 description 1
150000007522 mineralic acids Chemical class 0.000 description 1
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230000001590 oxidative effect Effects 0.000 description 1
239000006072 paste Substances 0.000 description 1
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NBIIXXVUZAFLBC-UHFFFAOYSA-K phosphate Chemical compound [O-]P([O-])([O-])=O NBIIXXVUZAFLBC-UHFFFAOYSA-K 0.000 description 1
239000010452 phosphate Substances 0.000 description 1
NBIIXXVUZAFLBC-UHFFFAOYSA-N phosphoric acid Substances OP(O)(O)=O NBIIXXVUZAFLBC-UHFFFAOYSA-N 0.000 description 1
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125000006308 propyl amino group Chemical group 0.000 description 1
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150000003254 radicals Chemical class 0.000 description 1
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238000010992 reflux Methods 0.000 description 1
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150000003343 selenium compounds Chemical class 0.000 description 1
FESBVLZDDCQLFY-UHFFFAOYSA-N sete Chemical compound [Te]=[Se] FESBVLZDDCQLFY-UHFFFAOYSA-N 0.000 description 1
239000004460 silage Substances 0.000 description 1
125000005624 silicic acid group Chemical class 0.000 description 1
235000012239 silicon dioxide Nutrition 0.000 description 1
235000009518 sodium iodide Nutrition 0.000 description 1
RYYKJJJTJZKILX-UHFFFAOYSA-M sodium octadecanoate Chemical compound [Na+].CCCCCCCCCCCCCCCCCC([O-])=O RYYKJJJTJZKILX-UHFFFAOYSA-M 0.000 description 1
235000010199 sorbic acid Nutrition 0.000 description 1
239000004334 sorbic acid Substances 0.000 description 1
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239000004455 soybean meal Substances 0.000 description 1
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235000000346 sugar Nutrition 0.000 description 1
150000008163 sugars Chemical class 0.000 description 1
HXJUTPCZVOIRIF-UHFFFAOYSA-N sulfolane Chemical compound O=S1(=O)CCCC1 HXJUTPCZVOIRIF-UHFFFAOYSA-N 0.000 description 1
239000001117 sulphuric acid Substances 0.000 description 1
235000011149 sulphuric acid Nutrition 0.000 description 1
239000013589 supplement Substances 0.000 description 1
239000000725 suspension Substances 0.000 description 1
239000003826 tablet Substances 0.000 description 1
239000003760 tallow Substances 0.000 description 1
YBRBMKDOPFTVDT-UHFFFAOYSA-N tert-butylamine Chemical compound CC(C)(C)N YBRBMKDOPFTVDT-UHFFFAOYSA-N 0.000 description 1
230000001988 toxicity Effects 0.000 description 1
231100000419 toxicity Toxicity 0.000 description 1
WBPYTXDJUQJLPQ-VMXQISHHSA-N tylosin Chemical compound O([C@@H]1[C@@H](C)O[C@H]([C@@H]([C@H]1N(C)C)O)O[C@@H]1[C@@H](C)[C@H](O)CC(=O)O[C@@H]([C@H](/C=C(\C)/C=C/C(=O)[C@H](C)C[C@@H]1CC=O)CO[C@H]1[C@@H]([C@H](OC)[C@H](O)[C@@H](C)O1)OC)CC)[C@H]1C[C@@](C)(O)[C@@H](O)[C@H](C)O1 WBPYTXDJUQJLPQ-VMXQISHHSA-N 0.000 description 1
229960004059 tylosin Drugs 0.000 description 1
235000019375 tylosin Nutrition 0.000 description 1
MWOOGOJBHIARFG-UHFFFAOYSA-N vanillin Chemical compound COC1=CC(C=O)=CC=C1O MWOOGOJBHIARFG-UHFFFAOYSA-N 0.000 description 1
FGQOOHJZONJGDT-UHFFFAOYSA-N vanillin Natural products COC1=CC(O)=CC(C=O)=C1 FGQOOHJZONJGDT-UHFFFAOYSA-N 0.000 description 1
235000012141 vanillin Nutrition 0.000 description 1
235000015112 vegetable and seed oil Nutrition 0.000 description 1
239000008158 vegetable oil Substances 0.000 description 1
235000013311 vegetables Nutrition 0.000 description 1
SYOKIDBDQMKNDQ-XWTIBIIYSA-N vildagliptin Chemical compound C1C(O)(C2)CC(C3)CC1CC32NCC(=O)N1CCC[C@H]1C#N SYOKIDBDQMKNDQ-XWTIBIIYSA-N 0.000 description 1
235000019165 vitamin E Nutrition 0.000 description 1
229940046009 vitamin E Drugs 0.000 description 1
239000011709 vitamin E Substances 0.000 description 1
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238000005303 weighing Methods 0.000 description 1
210000002268 wool Anatomy 0.000 description 1
JKQXZKUSFCKOGQ-QAYBQHTQSA-N zeaxanthin Chemical compound C([C@H](O)CC=1C)C(C)(C)C=1\C=C\C(\C)=C\C=C\C(\C)=C\C=C\C=C(/C)\C=C\C=C(/C)\C=C\C1=C(C)C[C@@H](O)CC1(C)C JKQXZKUSFCKOGQ-QAYBQHTQSA-N 0.000 description 1
239000011787 zinc oxide Substances 0.000 description 1

Classifications

- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D235/00—Heterocyclic compounds containing 1,3-diazole or hydrogenated 1,3-diazole rings, condensed with other rings
- C07D235/02—Heterocyclic compounds containing 1,3-diazole or hydrogenated 1,3-diazole rings, condensed with other rings condensed with carbocyclic rings or ring systems
- C07D235/04—Benzimidazoles; Hydrogenated benzimidazoles
- C07D235/06—Benzimidazoles; Hydrogenated benzimidazoles with only hydrogen atoms, hydrocarbon or substituted hydrocarbon radicals, directly attached in position 2
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D235/00—Heterocyclic compounds containing 1,3-diazole or hydrogenated 1,3-diazole rings, condensed with other rings
- C07D235/02—Heterocyclic compounds containing 1,3-diazole or hydrogenated 1,3-diazole rings, condensed with other rings condensed with carbocyclic rings or ring systems
- C07D235/04—Benzimidazoles; Hydrogenated benzimidazoles
- C07D235/06—Benzimidazoles; Hydrogenated benzimidazoles with only hydrogen atoms, hydrocarbon or substituted hydrocarbon radicals, directly attached in position 2
- C07D235/08—Radicals containing only hydrogen and carbon atoms
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D235/00—Heterocyclic compounds containing 1,3-diazole or hydrogenated 1,3-diazole rings, condensed with other rings
- C07D235/02—Heterocyclic compounds containing 1,3-diazole or hydrogenated 1,3-diazole rings, condensed with other rings condensed with carbocyclic rings or ring systems
- C07D235/04—Benzimidazoles; Hydrogenated benzimidazoles
- C07D235/06—Benzimidazoles; Hydrogenated benzimidazoles with only hydrogen atoms, hydrocarbon or substituted hydrocarbon radicals, directly attached in position 2
- C07D235/10—Radicals substituted by halogen atoms or nitro radicals
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D235/00—Heterocyclic compounds containing 1,3-diazole or hydrogenated 1,3-diazole rings, condensed with other rings
- C07D235/02—Heterocyclic compounds containing 1,3-diazole or hydrogenated 1,3-diazole rings, condensed with other rings condensed with carbocyclic rings or ring systems
- C07D235/04—Benzimidazoles; Hydrogenated benzimidazoles
- C07D235/24—Benzimidazoles; Hydrogenated benzimidazoles with hetero atoms or with carbon atoms having three bonds to hetero atoms with at the most one bond to halogen, e.g. ester or nitrile radicals, directly attached in position 2
- C07D235/26—Oxygen atoms

Landscapes

Chemical & Material Sciences (AREA)
Organic Chemistry (AREA)
Pharmaceuticals Containing Other Organic And Inorganic Compounds (AREA)
Plural Heterocyclic Compounds (AREA)
Organic Low-Molecular-Weight Compounds And Preparation Thereof (AREA)
Fodder In General (AREA)

PH38006A 1988-01-05 1989-01-05 Use of benzimidazole derivatives as yield promoters PH26142A (en)

Applications Claiming Priority (1)

Application Number	Priority Date	Filing Date	Title
DE3800096A DE3800096A1 (de)	1988-01-05	1988-01-05	Verwendung von benzimidazolderivaten als leistungsfoerderer

Publications (1)

Publication Number	Publication Date
PH26142A true PH26142A (en)	1992-03-18

Family

ID=6344829

Family Applications (1)

Application Number	Title	Priority Date	Filing Date
PH38006A PH26142A (en)	1988-01-05	1989-01-05	Use of benzimidazole derivatives as yield promoters

Country Status (15)

Country	Link
US (1)	US4960783A (cs)
EP (1)	EP0325802A1 (cs)
JP (1)	JPH02138264A (cs)
KR (1)	KR890011858A (cs)
AU (1)	AU2752888A (cs)
BR (1)	BR8900024A (cs)
CS (1)	CS9589A2 (cs)
DE (1)	DE3800096A1 (cs)
DK (1)	DK2489A (cs)
HU (1)	HU203324B (cs)
IL (1)	IL88847A0 (cs)
NZ (1)	NZ227460A (cs)
PH (1)	PH26142A (cs)
PL (1)	PL154143B1 (cs)
ZA (1)	ZA8941B (cs)

Families Citing this family (8)

* Cited by examiner, † Cited by third party
Publication number	Priority date	Publication date	Assignee	Title
PE27997A1 (es)	1994-04-29	1997-09-20	Lilly Co Eli	Antagonistas de receptores de taquicininas
ZA967892B (en) *	1995-09-21	1998-03-18	Lilly Co Eli	Selective β3 adrenergic agonists.
US6075040A (en) *	1996-09-05	2000-06-13	Eli Lilly And Company	Selective β3 adrenergic agonists
US5849826A (en)	1995-10-27	1998-12-15	Mitsui Petrochemical Industries, Ltd.	Semiaromatic polyamides, processes for preparing the same and compositions containing the same
ES2171839T3 (es)	1996-09-05	2002-09-16	Lilly Co Eli	Analogos de carbazol como agonistas adrenergicos selectivos de beta3.
CO5011072A1 (es) *	1997-12-05	2001-02-28	Lilly Co Eli	Etanolaminas pirazinil substituidas como agfonistas de los receptores
JP7682097B2 (ja)	2019-03-27	2025-05-23	キュラセンセラピューティクスインコーポレイテッド	ベータアドレナリンアゴニスト及びそれを使用する方法
TWI877182B (zh) *	2019-07-01	2025-03-21	美商古拉森療法公司	β腎上腺素激動劑及其使用方法

Family Cites Families (7)

* Cited by examiner, † Cited by third party
Publication number	Priority date	Publication date	Assignee	Title
FR3697M (fr) *	1963-05-27	1965-11-22	Ici Ltd	Médicaments a base de nouveaux composés hétérocycliques pour le traitement des maladies des arteres coronaires.
DE2432269A1 (de) *	1974-07-05	1976-01-22	Boehringer Mannheim Gmbh	Basisch substituierte derivate des 4-hydroxybenzimidazols und verfahren zu ihrer herstellung
CH624395A5 (cs) *	1976-01-08	1981-07-31	Ciba Geigy Ag
US4204069A (en) *	1976-12-06	1980-05-20	Merck & Co., Inc.	Reductive alkylation
US4082847A (en) *	1976-12-06	1978-04-04	Merck & Co., Inc.	Substituted aminoethanols and pharmaceutical use
US4070478A (en) *	1977-02-17	1978-01-24	Merck & Co., Inc.	Benzimidazole substituted alanines
DE3428526A1 (de) *	1984-08-02	1986-02-13	Boehringer Mannheim Gmbh, 6800 Mannheim	Neue aminoalkohole, verfahren zu deren herstellung sowie diese verbindung enthaltende arzneimittel

1988
- 1988-01-05 DE DE3800096A patent/DE3800096A1/de not_active Withdrawn
- 1988-12-22 NZ NZ227460A patent/NZ227460A/en unknown
- 1988-12-23 AU AU27528/88A patent/AU2752888A/en not_active Abandoned
- 1988-12-27 JP JP63328077A patent/JPH02138264A/ja active Pending
- 1988-12-30 IL IL88847A patent/IL88847A0/xx unknown
- 1988-12-30 EP EP88121880A patent/EP0325802A1/de not_active Withdrawn
- 1988-12-30 US US07/292,581 patent/US4960783A/en not_active Expired - Fee Related
1989
- 1989-01-04 ZA ZA8941A patent/ZA8941B/xx unknown
- 1989-01-04 PL PL1989277049A patent/PL154143B1/pl unknown
- 1989-01-04 DK DK002489A patent/DK2489A/da not_active Application Discontinuation
- 1989-01-04 BR BR898900024A patent/BR8900024A/pt unknown
- 1989-01-04 HU HU8922A patent/HU203324B/hu unknown
- 1989-01-05 KR KR1019890000023A patent/KR890011858A/ko not_active Withdrawn
- 1989-01-05 CS CS8995A patent/CS9589A2/cs unknown
- 1989-01-05 PH PH38006A patent/PH26142A/en unknown

Also Published As

Publication number	Publication date
DK2489D0 (da)	1989-01-04
KR890011858A (ko)	1989-08-23
US4960783A (en)	1990-10-02
JPH02138264A (ja)	1990-05-28
BR8900024A (pt)	1989-08-15
HUT49588A (en)	1989-10-30
AU2752888A (en)	1989-07-13
IL88847A0 (en)	1989-07-31
HU203324B (en)	1991-07-29
PL277049A1 (en)	1989-09-18
EP0325802A1 (de)	1989-08-02
DK2489A (da)	1989-07-06
CS9589A2 (en)	1991-08-13
PL154143B1 (en)	1991-07-31
NZ227460A (en)	1990-11-27
ZA8941B (en)	1989-09-27
DE3800096A1 (de)	1989-07-13

Publication	Publication Date	Title
PH26142A (en)	1992-03-18	Use of benzimidazole derivatives as yield promoters
HU192267B (en)	1987-05-28	Process for production of substituated 2-phenil-hexahydro-1,2,4-triasine-3,5-dions and veterinary preparatives containing thereof
US3493572A (en)	1970-02-03	Process for producing quinoxaline-di-n-oxides
DE3306160A1 (de)	1984-08-23	Wachstumsfoerdernde aminophenylethylamin-derivate
EP0301348B1 (de)	1993-02-03	Substituierte Pyridylethanolamine, Verfahren zu ihrer Herstellung und ihre Verwendung als Leistungsförderer bei Tieren
US4863939A (en)	1989-09-05	Heteroarylethylamine as production promoters in livestock
EP0209025B1 (de)	1988-09-28	Arylethanolhydroxylamine, Verfahren zu ihrer Herstellung und ihre Verwendung zur Leistungsförderung
JPS63295536A (ja)	1988-12-01	新規なアミノフエニルエチルアミン誘導体類、それらの製造方法および生産量増進剤としてのそれらの使用
DE2616646A1 (de)	1976-10-28	Verfahren und zusammensetzungen fuer die verwendung in der tierzucht
CS239937B2 (en)	1986-01-16	Processing of cycloalcane derivatives
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